Barefoot Walking VS Standardised Conservative Care for Plantar Fasciopathy
RecruitingNot applicableNCT07600229
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The goal of this clinical trial is to learn if a barefoot walking programme can treat plantar fasciopathy (heel pain) in adults aged 18-70. The main questions it aims to answer are: * Does a barefoot walking programme reduce heel pain compared to a standardised stretching and strengthening programme? * Does a barefoot walking programme improve foot function and quality of life in adults with plantar fasciopathy? Researchers will compare a barefoot walking programme to a standardised stretching and strengthening programme to see if barefoot walking is an effective conservative management approach for plantar fasciopathy. Participants will: * Be randomly assigned to either a barefoot walking programme or a stretching and strengthening programme * Complete a 12-week home-based exercise programme * Complete short weekly questionnaires throughout the 12 weeks * Complete 3 follow-up surveys over 6 months after the intervention ends * Receive education on load management and plantar fasciopathy
Study details
- Official title
- Clinical and Economic Effectiveness of Barefoot Walking Compared to Standardised Conservative Care for the Treatment of Plantar Fasciopathy: a Pragmatic Randomised Controlled Trial
- Conditions
- Plantar Fasciopathy
- Plantar Fasciitis
- Plantar Fasciitis, Chronic
- Heel Pain
- Interventions
- Behavioral: Barefoot Walking Programme
- Behavioral: Standardised Conservative Care
- Sponsor
- Elisabetta Brigo
- Organization
- South East Technological University
- Start date
- 2026-05-07
- Primary completion
- 2027-10-31
- Sex
- All
- Age range
- from 18 Years to 70 Years
- Results posted
- No results posted in this snapshot
- Countries
- Ireland
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Aged 18-70 years; * Clinical diagnosis of Plantar Fasciopahty, defined by: a) Pain localised to the medial calcaneal tubercle of sharp or stabbing quality; b) Pain worst with the first few steps in the morning or after a period of rest (first-step pain); c) Pain reproduced with palpation of the medial calcaneal tubercle OR positive Windlass Test; * Symptom duration greater than 4 weeks; * Able to walk independently without a mobility aid * Able to provide informed consent and comply with study protocol Exclusion Criteria: * Prior surgery on the affected foot * Diabetes with peripheral neuropathy or other neurological condition affecting lower limb sensation or motor control * Active inflammatory arthropathy, uncontrolled vascular disease, or inability to walk unaided * Current or recent (less than 6 months) bony stress fracture or other acute foot or ankle injury on the affected side * Pregnancy during the intervention period * BMI greater than 40 kg/m² * Corticosteroid injection to the affected foot within the previous 3 months * Night splints initiated less than 4 weeks prior to enrolment * Any condition that would make participation unsafe, including open foot wounds
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07600229